A self-contained, hyperthermic conditioning unit and selectively controllable environment for exercising. The unit comprises a base portion having a bed therein and a removable cover connected to the base portion to enclose a personal compartment within the unit. One or more heating elements provide heat to the personal compartment and one more pieces of physical exercise equipment are provided within the personal compartment.

A system and method for hyperthermic ablation of cancerous tissue of a human patient is disclosed. A system and method include a vessel that is sized and adapted for receiving the human patient, and a circulation device outside of the vessel for circulating a thermally conductive liquid to and from the vessel, such that the portion of the human patient enclosed in the containment suit is at least partially submerged in the thermally conductive liquid when the human patient is in the vessel. The system and method further include a set of electromagnetic transmission coils at least partially around the vessel for inducing an alternating electromagnetic field around the human patient, the alternating electromagnetic field being directed, via the thermally conductive liquid, to the cancerous tissue that has been provided a conductive nanoparticle, to provide hyperthermic ablation of the cancerous tissue.

Various systems and devices are provided for determining a weaning readiness for weaning a patient from a thermoregulated microenvironment. In one example, a method includes receiving current patient parameters of the patient and applying a weaning model to the current patient parameters to calculate a weaning index representing a likelihood that the patient can be successfully weaned from the microenvironment. The method also includes outputting the weaning index for display on a display device or for storage in a medical record of the patient and upon outputting the weaning index, receiving one or more subsequent patient outcomes, the one or more subsequent patient outcomes comprising whether the patient developed any complications within the duration since being weaned from the microenvironment. The method also includes updating the weaning model based on the one or more received subsequent patient outcomes.

A Cold Therapy Cooler Apparatus includes a port body with a flange and threads that is inserted into an orifice in the sidewall or lid of a cooler. An interior retaining ring with compatible threads cooperates with the flange to retain the port body within the orifice. A circulating pump is inside the cooler. An internal supply hose is connected to the pump, and to a supply pass-through that passes through the port body and is connected to an exterior supply hose. An internal return hose is connected to the pump, and to a return pass-through that passes through the port body and is connected to an exterior return hose. The exterior hoses are connected to an anatomical area cooling device. A power cord is connected to the pump and to a power cord connection by way of a power cord pass-through that passes through the port body.

The subject of the invention is a device for systemic cryotherapy with an engine room assembly (22) comprising a cryochamber and the engine room assembly (22), which comprises an upper inlet channel housing (8), which is connected, on the bottom, to a ventilation fitting housing (1) connected, on the bottom, to a heat exchanger (2) housing, wherein a cryogenic liquid supply (19) and cryogenic liquid vapour discharge (20) system is located on the side wall, and the lower flange of the heat exchanger (2) is connected to the lower outlet channel housing (3), and the device is connected to a power supply system, characterised in that the upper inlet channel housing (8) is L-shaped, and a duct fan (15) is located in the ventilation fitting housing (1), wherein a heater (9) is located between the ventilation fitting (1) and the heat exchanger (2).

In accordance with one embodiment, a uniform total body cryotherapy method and apparatus operative to allow an individual in a cryotherapy chamber to be subjected to the same cold temperatures on their entire body at the same time. In use, the apparatus allows active dissemination of cold air in a confined space without the undesired consequence of wind shear commonly caused by forced movement of cold air.

Various systems and devices are provided for determining a weaning readiness for weaning a patient from a thermoregulated microenvironment. In one example, a method includes receiving a plurality of current patient parameters of a patient housed in a thermoregulated microenvironment, applying a weaning model to the plurality of current patient parameters to generate a weaning index representing a likelihood that the patient will be successfully weaned from the microenvironment if weaned at that time, the weaning model trained to correlate the current patient parameters with the likelihood based on historical data of prior patients and known outcomes for those prior patients, and outputting the weaning index for display on a display device and/or for storage in a medical record of the patient.

In methods for treating a patient, a time varying magnetic field is applied to a patient's body and causes a muscle contraction. The time-varying magnetic field may be monophasic, biphasic, polyphasic and/or static. The method may reduce adipose tissue, improve metabolism, blood and/or lymph circulation. The method may use combinations of treatments to enhance the visual appearance of the patient.

A thermogenic emergency airway management device configured to prevent or treat hypothermia in a patient. The device may be configured to receive inlet air and modify one or more properties of the inlet air to output air at a temperature and/or humidity associated with the prevention and/or treatment of hypothermia. In an embodiment, the device may receive input via a user interface to determine a temperature and/or humidity associated with the air to be output to the patient. In an embodiment, the input may additionally include an amount of air to be output to the patient. In such an embodiment, the device may be configured to cause the amount of air to be output to the patient to prevent and/or treat hypothermia.

A thermal transfer device for providing thermal treatment to a patient. A patient support portion supporting and contacting the patient includes a first segment of a fluid flow path to receive a fluid from a fluid source. A flexible covering coupled and movable relative to the patient support portion defines a space therebetween that substantially conforms to the patient. The flexible covering includes a second segment of the fluid flow path. The fluid is circulated through an inlet, an outlet, and fluid flow path for supplying heat to or removing heat from the patient support portion and the flexible covering. A fluid circulation system with a controller may selectively adjust heat transfer from temperature zones defining the patient support portion. The thermal transfer device or a mattress cover may provide for controlling the microclimate, or conditions at or near the interface between the patient and the patient support portion.